Canonical Allele Identifier: CA491132870

Gene: GRAMD2A

Linked Data

• MyVariant Identifiers: chr15:g.72462256T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72169915T>G , CM000677.2:g.72169915T>G	GRCh38
NC_000015.9:g.72462256T>G , CM000677.1:g.72462256T>G	GRCh37
NC_000015.8:g.70249310T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000309731.12:c.66A>C MANE Select	ENSP00000311657.7:p.Thr22=
ENST00000309731.11:c.66A>C	ENSP00000311657.7:p.Thr22=
ENST00000562288.1:c.30A>C	ENSP00000457155.1:p.Thr10=
ENST00000563133.5:n.221A>C
ENST00000564129.5:c.36A>C	ENSP00000457660.1:p.Thr12=
ENST00000568594.5:c.45A>C	ENSP00000457383.1:p.Thr15=
ENST00000570275.5:c.30A>C	ENSP00000457088.1:p.Thr10=
NM_001012642.2:c.66A>C	NP_001012660.1:p.Thr22=
XM_011521327.1:c.63A>C	XP_011519629.1:p.Thr21=
XM_011521328.1:c.60A>C	XP_011519630.1:p.Thr20=
XM_011521329.1:c.36A>C	XP_011519631.1:p.Thr12=
XM_011521330.1:c.30A>C	XP_011519632.1:p.Thr10=
XM_011521331.1:c.66A>C	XP_011519633.1:p.Thr22=
XM_011521332.1:c.-190A>C	XP_011519634.1:n.-190A>C
XM_011521333.1:c.-190A>C	XP_011519635.1:n.-190A>C
XM_011521327.2:c.63A>C	XP_011519629.1:p.Thr21=
XM_011521328.3:c.60A>C	XP_011519630.1:p.Thr20=
XM_011521329.2:c.36A>C	XP_011519631.1:p.Thr12=
XM_011521330.2:c.30A>C	XP_011519632.1:p.Thr10=
XM_011521331.2:c.66A>C	XP_011519633.1:p.Thr22=
XM_011521332.3:c.-190A>C	XP_011519634.1:n.-190A>C
XM_011521333.3:c.-190A>C	XP_011519635.1:n.-190A>C
XM_017021997.1:c.-174A>C	XP_016877486.1:n.-174A>C
XM_017021998.1:c.-174A>C	XP_016877487.1:n.-174A>C
XM_024449868.1:c.15A>C	XP_024305636.1:p.Thr5=
NM_001012642.3:c.66A>C MANE Select	NP_001012660.1:p.Thr22=